Senior Clinical Data Analytics & Reporting Programmer

About the Role We are seeking an experienced Clinical Data Analytics & Reporting Programmer to lead the development of advanced analytics, reporting, and data visualization solutions supporting global clinical trials. This role partners with cross-functional stakeholders to transform complex clinical data into actionable insights that drive medical monitoring, risk-based monitoring, data review, and clinical decision‑making initiatives.

• Lead the design, development, and delivery of clinical reporting, dashboards, visualizations, metrics, and analytical solutions.
• Partner with business stakeholders to gather requirements and translate them into scalable reporting and analytics solutions.
• Mentor team members and provide technical leadership on reporting, visualization, and analytics best practices.
• Drive process improvements and innovative approaches to clinical data reporting and analytics.
• Serve as a subject matter expert for clinical data analytics, visualization platforms, and reporting technologies.
• Independently manage complex assignments and deliver high-quality solutions with minimal oversight.

• Bachelor's degree in Computer Science, Engineering, Statistics, Life Sciences, or a related discipline.
• 4+ years of experience as a Business Analyst, Clinical Data Analyst, or similar analytics‑focused role working with data warehouse environments in a regulated industry and clinical trial setting.
• Advanced expertise in data visualization and dashboard development using TIBCO Spotfire or comparable business intelligence platforms.
• Strong programming experience with Python, R, SAS, or similar analytical scripting languages.
• Experience gathering business requirements and developing user requirements documentation.
• Strong understanding of clinical trial data structures, including SDTM.

• 6+ years of relevant experience in clinical data analytics, reporting, or business intelligence within pharmaceutical, biotechnology, or life sciences organizations.
• Knowledge of CDISC standards and clinical data standards implementation.
• Experience mentoring, coaching, and developing junior team members.
• Demonstrated ability to apply advanced technical and problem‑solving skills to deliver innovative solutions that improve operational efficiency.
• Experience serving as a technical subject matter expert in clinical data analytics, reporting, or therapeutic area‑specific domains.

• The ideal candidate combines deep technical expertise in clinical data analytics with strong stakeholder engagement skills.
• You thrive in highly regulated environments, can independently solve complex business challenges, and have a proven track record of delivering impactful reporting and visualization solutions that support clinical development and decision‑making.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material…